Compound Middle Lamella Regions Research Articles

Changes of Chemical Composition and Hemicelluloses Structure in Differently Aged Bamboo ( Neosinocalamus affinis) Culms.

To study the differences in chemical composition analysis and spatial distribution of young Neosinocalamus affinis bamboo, we used the methods of standard of National Renewable Energy Laboratory and confocal Raman microscopy, respectively. It was found that the acid-soluble lignin and acid-insoluble lignin content showed an inverse relationship with the increasing bamboo age. Raman analysis revealed that Raman signal intensity of lignin in both the secondary cell wall and the compound middle lamella regions showed a similar increase trend with growth of bamboo. In addition, eight hemicellulosic fractions were obtained by successively treating holocellulose of the 2-, 4-, 8-, and 12-month-old Neosinocalamus affinis bamboo culms with DMSO and alkaline solution. The ratio of arabinose to xylose of hemicelluloses was increased with the growth of bamboo. FT-IR and NMR analyses revealed that DMSO-soluble hemicelluloses of young bamboo culms are mainly composed of highly substituted xylans and β-d-glucans.

Oak wood inhabiting fungi and their effect on lignin studied by UV microspectrophotometry

Decayed-wood samples were collected from a naturally-infected bridge made of Quercus robur. Fruiting bodies of the white-rot basidiomycetes Hymenochaete rubiginosa and Stereum hirsutum were sampled. The white-rot fungus Fuscoporia ferrea and the secondary saprobiont Mycena galericulata were identified from the rotten wood by means of rDNA-ITS sequencing. The topochemistry of lignin degradation within individual cell-wall layers was determined by cellular UV-microspectrophotometry (UMSP) at 278 nm wavelength. Increased delignification occurred in compound middle lamella regions (CML), secondary wall layers of fibres (S2), longitudinal and ray parenchyma cells as well in vessels. The highest lignin content at initial and medium decay was recorded in the CML, whereas in advanced decay secondary wall layers of the vessels exhibited the highest content of residual lignin. In all stages of degradation, the S2 layers of fibres had the lowest lignin amount.

Proposed supramolecular structure of lignin in softwood tracheid compound middle lamella regions

Abstract The structure of lignin in the compound middle lamella (CML) of softwood tracheids differs from that in the secondary wall (SW) in regard to the content of condensed structures (5-5′-biphenyl, dibenzodioxocin and 4-O-5′-diphenyl ether). In an early stage of cell wall formation, random coarse networks composed of thin cellulose microfibrils (CMFs), hemicelluloses, and pectin are formed in the CML, then globular p-hydroxyphenyl/guaiacyl lignin (HG-lignin) is deposited quickly into the network. The globular lignin is assumed to be a micellar aggregate of oligolignols folded at the β-O-4 bond with their phenolic ends on the outer part of the aggregate. When 3D clusters of the globules are deposited on the preformed network of polysaccharides, further growth of the oligolignols by endwise addition of new monolignols is spatially limited, so frequent condensation occurs between growing aromatic ends of adjacent HG-oligolignols within the globule and between the wide contact boundaries of the 3D clustered globules to produce a highly condensed supramolecule in CML. In SW, the folded G-oligolignols are deposited slowly in the narrow tubular space surrounding thick CMFs coated with hemicelluloses. Condensation occurs mostly between adjacent growing ends of the oligolignols within the tubular aggregates. Spatial regulation of condensation of folded polylignols is one of the factors producing a different supramolecular structure for CML lignin than for SW lignin.

Topochemical investigation into the delignification of Eucalyptus globulus chips during semi-chemical sulfite pulping

The course of delignification of Eucalyptus globulus fibers during neutral semi-chemical sulfite pulping (NSSC) was studied by universal microspectrophotometry (UMSP 80, ZEISS). UV-investigation into a cellular level enables the topochemical analyses of delignification within individual cell wall layers during cooking. Cooks were carried out in a laboratory seven liter digester with liquor circulation and electrical heating device. Chip samples were taken throughout the cooking for chemical and UV microscopic analyses. UV microscopy analysis revealed for Eucalyptus globulus chips a preferred lignin removal during NSSC cooking in cell corner and compound middle lamella regions.

Tensile growth stress and lignin distribution in the cell walls of yellow poplar, Liriodendron tulipifera Linn.

Five specimens that contained a continuous gradient of wood, from normal to tension wood regions, were collected from an inclined yellow poplar (Liriodendron tulipifera), and the released strain of tensile growth stress was quantified. Ultraviolet (UV) microspectrophotometry was used to examine the relationship between lignin distribution in the cell wall and the intensity of tensile growth stress. The UV absorption of the secondary wall and the cell corner middle lamella decreased with increasing tensile released strain (i.e., tensile growth stress). The UV absorption in the compound middle lamella region remained virtually constant, irrespective of the tensile released strain. The absorption maximum (λmax) remained virtually constant in the secondary wall, the cell corner middle lamella, and the compound middle lamella region at 273–274, 277–278, and 275–278 nm respectively, irrespective of the tensile released strain. The ratios of the UV absorbance at 280 to 260 nm and 280 to 273 nm of the secondary wall decreased with increasing tensile released strain. The ratios in the cell corner and compound middle lamella region remained constant, irrespective of the tensile released strain. The lignin content of the secondary wall decreased, while the syringyl/guaiacyl ratio increased with increasing tensile released strain. Gelatinous fibers were not observed in the tension wood regions, but the secondary wall became gelatinous-layer-like, i.e., the lignin content and microfibrillar angle decreased and the cellulose content increased. A definite gelatinous layer seems to be important for generating greater tensile growth stress. It is concluded that a decrease in lignin and an increase in cellulose microfibrils parallel to the fiber axis in the secondary wall are necessary to produce large tensile growth stress.

Heterogeneity in Formation of Lignin. XIII. Formation of p-Hydroxyphenyl Lignin in Various Hardwoods Visualized by Microautoradiography

Abstract The heterogeneous nature of hardwood lignin was shown by visualizing the deposition process of p-hydroxyphenyl (H) lignin in the differentiating xylem of magnolia, beech, lilac and poplar. When p-glucocoumaryl alcohol-[arom. ring-2-3H], an efficient precursor of H units in lignin, was administered to the differentiating xylem of these trees, radioactivity was incorporated in the compound middle lamella region of vessel and fiber cell walls. The deposition of H units occurs only in the early stage of cell wall formation when the outer layer of the secondary wall is formed. H lignin deposits mainly within pectic substances and hemicellulose gel to form a highly condensed structural moiety.

Degradation of carbohydrates and lignins in buried woods

Spruce, alder, and oak woods deposited in coastal sediments were characterized versus their modern counterparts by quantification of individual neutral sugars and lignin-derived phenols as well as by scanning electron microscopy, 13C NMR, and elemental analysis. The buried spruce wood from a 2500 yr old deposit was unaltered whereas an alder wood from the same horizon and an oak wood from an open ocean sediment were profoundly degraded. Individual sugar and lignin phenol analyses indicate that at least 90 and 98 wt% of the initial total polysaccharides in the buried alder and oak woods, respectively, have been degraded along with 15–25 wt% of the lignin. At least 75% of the degraded biopolymer has been physically lost from these samples. This evidence is supported by the SEM, 13C NMR and elemental analyses, all of which indicate selective loss of the carbohydrate moiety. The following order of stability was observed for the major biochemical constituents of both buried hardwoods: vanillyl and p- hydroxyl lignin structural units > syringyl lignin structural units > pectin > α-cellulose > hemicellulose. This sequence can be explained by selective preservation of the compound middle lamella regions of the wood cell walls. The magnitude and selectivity of the indicated diagenetic reactions are sufficient to cause major changes in the chemical compositions of wood-rich sedimentary organic mixtures and to provide a potentially large in situ nutrient source.

A study of lignification in loblolly pine tracheids by the SEM-EDXA technique

The lignification process in different morphological regions of loblolly pine tracheids was studied by the SEM-EDXA technique. Prior to S2 layer formation, lignification was initiated in the cell corner middle lamella and compound middle lamella regions. Subsequently a rapid lignin deposition was observed in both regions, whereas secondary wall lignification was a more gradual process and initiated when the middle lamella lignin concentration was approximately 50% of maximum. Within the secondary wall, the S1 layer is lignified first. Then, lagging just behind cell wall formation, lignification of the S2 layer is initiated adjacent to the S1 layer and extends toward the lumen. Finally, the S3 layer lignified. Upon completion of lignification, the cell walls had a higher concentration of lignin in both the S1 and S3 layers than in the S2 layer.